Package 70436-018-06

Brand: olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide

Generic: olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 70436-018-06
Digits Only 7043601806
Product NDC 70436-018
Description

90 TABLET, FILM COATED in 1 BOTTLE (70436-018-06)

Marketing

Marketing Status
Marketed Since 2025-05-15
Brand olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide
Generic olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d306cb9e-4244-49dd-9297-9cb6ca69cae9", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0370436018048", "0370436016044", "0370436014040", "0370436015047", "0370436017041"], "unii": ["0J48LPH2TH", "864V2Q084H", "6M97XTV3HD"], "rxcui": ["999967", "999986", "999991", "999996", "1000001"], "spl_set_id": ["a469adff-25a6-4983-b471-60924d920a86"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Slate Run Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (70436-018-04)", "package_ndc": "70436-018-04", "marketing_start_date": "20250515"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (70436-018-06)", "package_ndc": "70436-018-06", "marketing_start_date": "20250515"}], "brand_name": "olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide", "product_id": "70436-018_d306cb9e-4244-49dd-9297-9cb6ca69cae9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A Inhibitors [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "70436-018", "generic_name": "olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide", "labeler_name": "Slate Run Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "10 mg/1"}, {"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "OLMESARTAN MEDOXOMIL", "strength": "40 mg/1"}], "application_number": "ANDA210718", "marketing_category": "ANDA", "marketing_start_date": "20250515", "listing_expiration_date": "20261231"}